J. Bella, J. Maccluer, M. Roman, L. Almasy, K. North, T. Welty, Elisa Lee, R. Fabsitz, B. Howard, R. Devereux
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In a polygenic model, the variables entered and identified as covariates of larger aortic root diameter were older age, male sex, and center (P <0.001), which accounted for 35% of the overall variability of aortic root diameter. After simultaneous adjustment was made for these significant covariates, the proportion of phenotypic variance due to additive genetic contribution or residual heritability (h2) was 0.51 (SE=0.08, P <0.001). Additionally, simultaneous adjustment for height, weight, and systolic and diastolic BPs yielded slightly lower residual h2 of aortic root diameter (h2=0.44, SE=0.08, P <0.001), which accounted for 26% of the overall variance of aortic root size. Because center effects were identified as significant covariates in the analyses, h2 analyses were performed separately in Arizona, Oklahoma, and North/South Dakota centers, which confirmed that a significant proportion of the phenotypic variance of aortic root diameter is due to additive genetic contribution. 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引用次数: 35
摘要
主动脉根部扩张是主动脉反流的主要病理生理机制,它使主动脉根部容易剥离或破裂。然而,只有一小部分主动脉根大小的差异可以用已知的临床和人口学相关因素来解释。本研究旨在确定美国印第安人参加第二次强心脏研究检查的超声心动图得出的主动脉根直径的遗传性。对1373名家庭成员≥1名的SHS参与者进行超声心动图分析。遗传力计算采用在SOLAR(一个计算机分析程序)中实现的方差成分分析。在多基因模型中,进入并确定为主动脉根直径较大协变量的变量是年龄较大、男性性别和中心(P <0.001),占主动脉根直径总体变异性的35%。在对这些显著协变量进行同步调整后,由加性遗传贡献或剩余遗传力(h2)引起的表型变异比例为0.51 (SE=0.08, P <0.001)。此外,同时调整身高、体重、收缩期和舒张期血压,主动脉根部直径的剩余h2略低(h2=0.44, SE=0.08, P <0.001),占主动脉根部大小总方差的26%。由于中心效应在分析中被确定为重要的协变量,因此在亚利桑那州、俄克拉荷马州和北达科他州/南达科他州的研究中心分别进行了h2分析,这证实了主动脉根直径表型变异的很大一部分是由于加性遗传贡献。遗传解释了主动脉根部大小变异的很大一部分,而这种变异与年龄、性别、体型和血压无关。超声心动图筛查有主动脉根部扩张的家庭成员可以识别其他易患主动脉夹层或破裂的个体。
Genetic Influences on Aortic Root Size in American Indians: The Strong Heart Study
Aortic root dilatation is a major pathophysiological mechanism for aortic regurgitation and predisposes the aortic root to dissection or rupture. However, only a small proportion of the variance of aortic root size can be explained by its known clinical and demographic correlates. The present study was undertaken to determine the heritability of echocardiographically derived aortic root diameter in the American Indian participants in the second Strong Heart Study examination. Echocardiograms were analyzed in 1373 SHS participants who had ≥1 family member in the cohort. Heritability calculations were performed by using variance component analysis as implemented in SOLAR, a computer analysis program. In a polygenic model, the variables entered and identified as covariates of larger aortic root diameter were older age, male sex, and center (P <0.001), which accounted for 35% of the overall variability of aortic root diameter. After simultaneous adjustment was made for these significant covariates, the proportion of phenotypic variance due to additive genetic contribution or residual heritability (h2) was 0.51 (SE=0.08, P <0.001). Additionally, simultaneous adjustment for height, weight, and systolic and diastolic BPs yielded slightly lower residual h2 of aortic root diameter (h2=0.44, SE=0.08, P <0.001), which accounted for 26% of the overall variance of aortic root size. Because center effects were identified as significant covariates in the analyses, h2 analyses were performed separately in Arizona, Oklahoma, and North/South Dakota centers, which confirmed that a significant proportion of the phenotypic variance of aortic root diameter is due to additive genetic contribution. Heredity explains a substantial proportion of the variability of aortic root size that is not accounted for by age, sex, body size, and blood pressure. Echocardiographic screening of family members with aortic root dilatation may identify other individuals predisposed to aortic dissection or rupture.